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. 2023 Mar 27;3(3):489–500. doi: 10.1158/2767-9764.CRC-22-0423

FIGURE 3.

FIGURE 3

AZD5305 potentiates the effect of CPT, causing significant and sustained regression of HOC106 tumors. A, Relative tumor volume (mean ± SEM) of HOC106 tumors growing subcutaneously. Tumor-bearing mice were randomized at a tumor volume of 185 mm3 (SD 54.2) to be treated with CPT (20 or 35 mg/kg i.v., once a week for 4 weeks) or AZD5305 (1 mg/kg orally every day, 5 days ON and two OFF for 8 weeks) or combination therapy: 4 weeks of concurrent treatment followed by 4 weeks of AZD5305 single agent (maintenance). Colored bars and arrows indicate the dosing periods. Number of mice/group = 6–7. Statistical significance of the combination versus the matching CPT monotherapy was analyzed as specified in Materials and Methods. *, P < 0.05; **, P ≤ 0.01; ***, P ≤ 0.005. B, Treatment efficacy expressed as the percentage of change in tumor volume (compared with the volume at treatment start) after 4 weeks of concurrent treatment (day 28), at the end of the therapy (day 56) and 4 weeks after treatment discontinuation (day 84). Each vertical bar in the waterfall plot represents a single mouse/tumor. Stable disease according to RECIST is highlighted in gray (from +20% to −30%). § Mouse euthanized when the volume considered a predefined endpoint (1,500 mm3) was reached.